|Study location||Austria, Linz|
|Type||Master courses, full-time|
|Nominal duration||2 years|
Undergraduate diploma (or higher)
Technical-scientific bachelor’s or diploma degree programme in engineering with 180 ECTS points or more.
You should prove at least 120 ECTS points in engineering courses of medical engineering/medical device technology.
The entry qualification documents are accepted in the following languages: English / German.
Often you can get a suitable transcript from your school. If this is not the case, you will need official translations along with verified copies of the original.
International applicants have to provide legalized copies of the documents in German or English. Legalisation must be done by the Austrian diplomatic representation.
TOEFL minimum score Internet-Based Test 78.
A motivation letter must be added to your application.
Advanced programming skills (Java, C/C++)
Please also attach the following documents:
Note that and interview and an entrance test is apart of the admission procedure.
The consecutive master’s degree programme Medical Engineering trains students to act as engineers with the ability to develop medical and rehabilitation devices in the regulatory framework of European and US-markets.
Enhanced education is provided by a project work and a master’s thesis, where students can apply their knowledge and problem solving abilities in a new or unfamiliar environment. In one part of the final diploma examination the students have to communicate their conclusions, and they show knowledge and rationale underpinning it.
The master’s degree program Medical Engineering qualifies students to work as engineers with the ability to develop medical and rehabilitation devices within the regulatory framework of European markets, and the ability to consider FDA regulations.
Graduates are able to work as engineers for the development and placement of medical devices, their maintenance or as product managers. They can also function as application specialists, advisors for medical products, in the licensing of medical products, and participate in quality management in project development, project leadership and strategy development on a national or international level.